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Diverse Functional Consequences of Mutations in the Na(+)/K(+)-ATPase α(2)-Subunit Causing Familial Hemiplegic Migraine Type 2
Mutations in ATP1A2, the gene coding for the Na(+)/K(+)-ATPase α(2)-subunit, are associated with both familial hemiplegic migraine and sporadic cases of hemiplegic migraine. In this study, we examined the functional properties of 11 ATP1A2 mutations associated with familial or sporadic hemiplegic mi...
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| Hlavní autoři: | , , , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
American Society for Biochemistry and Molecular Biology
2008
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2662176/ https://ncbi.nlm.nih.gov/pubmed/18728015 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.M802771200 |
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